Hemostatic device

ABSTRACT

A hemostatic device includes a covering member for covering a dorsal side of a patient&#39;s hand, the covering member including a hole through which a puncture site on the hand where bleeding is to be stopped, is exposed. The hemostatic device further includes a pressing member configured to apply a compression force to the puncture site when the pressing member is positioned over the site and fixed to the covering member, a fixing member configured to fix the pressing member to the covering member, and a support member configured to support the hand when the pressing member applies the compression force to the puncture site. At least a portion of the support member faces the hole portion with the hand interposed therebetween, when the covering member is disposed on the dorsal side of the hand.

CROSS-REFERENCE TO RELATED APPLICATION(S)

This application is a continuation of International Patent Application No. PCT/JP2019/013314, filed on Mar. 27, 2019, which is based upon and claims the benefit of priority from Japanese Patent Application No. 2018-069380, filed on Mar. 30, 2018, the entire contents of which are incorporated herein by reference.

FIELD

One or more embodiments disclosed herein relate to a hemostatic device.

BACKGROUND

As one of catheter procedures, a procedure of puncturing a blood vessel (for example, radial artery) of an arm of a patient to introduce various medical elongated bodies into the blood vessel via the puncture site formed in the blood vessel of the arm of the patient and performing a procedure or a treatment on a lesion site is disclosed in JP-A-2008-119517.

The radial artery extending along an arm of a human body is connected to a palmar artery. Accordingly, in recent years, a catheter procedure using distal transradial intervention (dTRI) in which the palmar artery located in the hand is punctured and treatment is performed through the puncture site, has been attempted.

The palmar artery is located in the hand and the hand has many movable portions such as fingers. Therefore, after a catheter procedure is performed in which the palmar artery is punctured, when an operator treats the puncture site located in a hand of a patient for hemostasis, it may be difficult to appropriately apply compression to the puncture site by existing hemostatic devices, which are for the arm or the leg. Therefore, a hemostatic device capable of effectively applying compression to the puncture site on the hand is desired.

When the puncture site is on the hand instead of the arm or the leg, since the hand has many movable portions such as fingers, it is difficult to fix the hemostatic device to the puncture site. Accordingly, the hemostatic device for supporting hemostasis on the puncture site on the hand needs to be positioned so that a pressing portion by which a compression force is applied to the puncture site is not displaced from the puncture site. In particular, when a patient extends or closes the hand, the shape of the hand is easily changed. Therefore, the hemostatic device for supporting hemostasis on the puncture site on the hand may be easily displaced, when the patient moves his or her hand. Accordingly, while using the hemostatic device for supporting hemostasis on the puncture site on the hand, it is important to appropriately maintain the compression force to the puncture site even when there is movement of the hand or the like.

SUMMARY

In consideration of the above-described problems, embodiments provide a hemostatic device capable of being easily fixed to a site of the hand where bleeding is to be stopped and maintaining a compression force that is applied by a pressing member to the site where the bleeding is to be stopped.

According to an embodiment, there is provided a hemostatic device including: a covering member configured to cover a dorsal side of a hand of a patient, the covering member including a hole portion through which a site on the dorsal side of the hand of the patient where bleeding is to be stopped, is to be exposed; a pressing member configured to apply a compression force to the site where the bleeding is to be stopped when the pressing member is positioned over the site and fixed to the covering member; a fixing member configured to fix the pressing member to the covering member; and a support member configured to support the hand of the patient when the pressing member applies the compression force to the site where the bleeding is to be stopped. At least a portion of the support member faces the hole portion with the hand interposed therebetween, when the covering member is disposed on the dorsal side of the hand.

The hemostatic device according to one or more embodiments includes the support member and the hole portion which exists at the position facing the support member with the hand interposed therebetween. Accordingly, the support member supports the pressing force applied to the puncture site where bleeding is to be stopped and which is surrounded by the hole portion. In addition, when the operator positions the pressing member at the puncture site of the hand, even though the puncture site exists in the hand having many movable portions such as fingers, the support member suppresses the movement of the pressing member in the vicinity of the puncture site. Therefore, the operator can easily mount the hemostatic device on the patient and position the pressing member at the puncture site of the hand. Moreover, in the hemostatic device, the support member exists at the position facing the hole portion on which the pressing member is positioned.

Accordingly, while hemostasis is progressing on the puncture site of the hand having many movable portions such as fingers, the support member supports a force from the dorsal side of the hand caused by the pressing member, and thus, the support member can suppress the displacement of the pressing member caused by the movement of the hand while supporting the compression force applied by the pressing member. In addition, when the operator mounts the hemostatic device on the patient, the hole portion exists at a position facing the support member. Accordingly, when the operator disposes the hole portion on the puncture site, the support member becomes positioned on the palm side of the puncture site, and thus, the operator can easily mount the hemostatic device on the patient.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 is a schematic perspective view of a hemostatic device according to an embodiment.

FIG. 2 is a perspective view illustrating a first state of the hemostatic device according to the embodiment that is mounted on a hand of a patient.

FIG. 3 is a perspective view illustrating a second state of the hemostatic device according to the embodiment that is mounted on the hand of the patient.

FIG. 4 is a plan view showing a palm side of the hemostatic device according to the embodiment when it is mounted on the hand of the patient.

FIG. 5 is an enlarged cross-sectional view of the hemostatic device taken along line 5A-5A illustrated in FIG. 3.

DESCRIPTION OF EMBODIMENTS

Hereinafter, one or more embodiments will be described with reference to the accompanying drawings. The following description is not intended to limit the technical scope and definitions of the terms described in the claims. In addition, dimensional ratios in the drawings may be exaggerated for convenience of explanation, and may be different from the actual ratios.

FIG. 1 is a view illustrating a hemostatic device 10, FIGS. 2 and 3 are views illustrating a procedure for mounting the hemostatic device 10 on a hand of a patient. FIG. 4 is a plan view of the hemostatic device 10 when it is mounted on the hand H of the patient and viewed from a palm Hp side, and FIG. 5 is an enlarged cross-sectional view of the hemostatic device 10 taken along line 5A-5A illustrated in FIG. 3. The hand H of the patient is not illustrated in FIG. 5.

For example, as illustrated in FIGS. 2 and 3, the hemostatic device 10 can be used to support hemostasis on a puncture site t1 after an elongated medical device (for example, introducer) indwelling in the puncture site t1 (corresponding to a “site where bleeding is to be stopped”) is removed from the puncture site t1. The puncture site t1 is formed on a radial artery side (for example, a distal radial artery extending around a snuff box or to a fingertip side from the snuff box) of a palmar artery (deep palmar artery) extending to a dorsal side Hb of the hand H of the patient. In the description of the embodiment, an example in which the hemostatic device 10 is used to support the hemostasis on the puncture site t1 formed in a left hand of the patient is described, but the hand targeted for use of the hemostatic device 10 may be a right hand.

FIG. 1 illustrates a perspective view of the hemostatic device 10 in a state before the hemostatic device 10 is mounted on the hand H of the patient.

In the following description, a distal side of a covering member 110 is a side located on a fingertip side of each of fingers f1 to f5 when the hemostatic device 10 is mounted on the hand H of the patient, and a proximal side of the covering member 110 is a side located on a forearm A side (wrist side) when the hemostatic device 10 is mounted on the hand H of the patient. In FIG. 4, the distal side is an upper side of the drawing and the proximal side is a lower side of the drawing.

As illustrated in FIGS. 1 and 3, the hemostatic device 10 includes the covering member 110 having a hole portion 115 at the puncture site t1 of the dorsal side Hb of the hand H of the patient, a pressing member 140 configured to apply a compression force to the puncture site t1 in a state (state illustrated in FIG. 3) where the hole portion 115 is at the puncture site t1, a fixing member 150 configured to fix the pressing member 140 to the covering member 110 in a state where the pressing member 140 is disposed on the hole portion 115, and a support member 160 (refer to FIG. 5) configured to support the hand H of the patient H when the pressing member 140 applies the compression force to the puncture site t1.

The hemostatic device 10 is disposed such that at least a portion of the support member 160 faces the hole portion 115 with the dorsal side Hb of the hand H of the patient interposed therebetween, in the state where the covering member 110 is disposed on the dorsal side Hb of the hand H of the patient. That is, in a state where the covering member 110 is disposed on the dorsal side Hb of the hand H of the patient, at least a portion of the support member 160 is disposed so as to overlap the hole portion 115 in the plan view illustrated in FIG. 4.

As illustrated in FIGS. 1 to 3, the covering member 110 is formed of a bag body 120 that is arranged so as to wrap the entire dorsal side Hb of the hand H while the covering member 110 is in contact with the dorsal side Hb of the hand H of the patient.

The bag body 120 has an internal space 124 (refer to FIG. 5) into which the hand H of the patient can be inserted, a first opening portion 121 through which fingers f1 to f4 (little finger f1, ring finger f2, middle finger f3, and forefinger f4) protrude from a distal side of the bag body 120 in a state where the hemostatic device 10 is mounted on the hand H of the patient, a second opening portion 122 through which a thumb f5 protrudes from the distal side of the bag body 120 in the state where the hemostatic device 10 is mounted on the hand H of the patient, and a third opening portion 123 through which the hand H passes when the hand H of the patient is inserted into the bag body 120.

As illustrated in FIGS. 2 and 3, the bag body 120 includes a first region 111, and a second region 112 which has elasticity lower than that of the first region 111. The second region 112 is arranged in a circumferential direction of the hand H of the patient passing by the hole portion 115 in a state where the hemostatic device 10 is mounted on the hand H of the patient.

As illustrated in FIG. 2, the first region 111 is arranged to wrap the hand H on the distal side of the covering member 110 from a root of each of the fingers f1 to f4. Moreover, the first region 111 is arranged to wrap a portion of the thumb f5 on the distal side from a root of the thumb f5. In addition, the first region 111 includes a finger hooking portion 125 which covers an interdigital space (finger spacing) between the forefinger f4 and the thumb f5.

In the hemostatic device 10, as illustrated in FIG. 3, in the state where the hemostatic device 10 is mounted on the hand H of the patient, each of the fingers f1 to f4 protrudes from the first opening portion 121 of the first region 111, and the thumb f5 protrudes from the second opening portion 122 of the first region 111. Accordingly, even during hemostasis supported by the hemostatic device 10, the patient can move each of the fingers f1 to f5. Moreover, in the hemostatic device 10, even when the fingers f1 to f5 move, it is possible to suppress displacement of the hemostatic device 10 by the finger hooking portion 125.

As illustrated in FIG. 2, the bag body 120 includes a third region 113 on a proximal side of the second region 112. The third region 113 is arranged to wrap the wrist and a portion of the forearm A of the patient when the hemostatic device 10 is mounted on the hand H of the patient.

As illustrated in FIG. 1, the covering member 110 includes a slit 116 which is formed across the third region 113 and the second region 112. The slit 116 is formed to connect a peripheral portion (a periphery of a proximal end of the third region 113) 123 of the covering member 110 to the hole portion 115. When an operator mounts the hemostatic device 10 on the hand H of the patient, the operator widens the slit 116, and thus, the hand H of the patient can be easily inserted into the internal space 124 of the bag body 120.

As illustrated in FIGS. 2 and 3, the covering member 110 has a restriction member 118 which suppresses enlargement of the slit 116. The restriction member 118 includes a first connection portion 118 a which is formed in the third region 113, and a second connection portion 118 b which is formed on a belt portion 126 attached to the third region 113.

For example, the first connection portion 118 a can be configured as the female side (or male side) of a surface fastener, and for example, the second connection portion 118 b can be configured as the male side (or female side) of the surface fastener. However, a specific structure of each of the connection portions 118 a and 118 b is not particularly limited as long as each connection portion has a structure that can be connected and separated.

The first connection portion 118 a and the second connection portion 118 b are connected to each other in the state where the hemostatic device 10 is mounted on the hand H of the patient, and thus, the restriction member 118 suppresses the enlargement of the slit 116. The hemostatic device 10 suppresses the enlargement of the slit 116 after the hemostatic device 10 is mounted on the patient, and thus, it is possible to prevent the covering member 110 from being displaced. Moreover, in the hemostatic device 10, the first connection portion 118 a and the second connection portion 118 b are connected to each other, and thus, the third region 113 of the bag body 120 can be fastened to the forearm A of the patient. Accordingly, the hemostatic device 10 can be appropriately mounted according to a thickness of the forearm A of the patient, and thus, the covering member 110 can be further prevented from being displaced.

As illustrated in FIG. 5, the second region 112 of the bag body 120 has a portion 112 a covering the dorsal side of the hand and a portion 112 b covering a palm side of the hand, and the portions 112 a and 112 b form the internal space 124 of the bag body 120. The hole portion 115 is formed in the portion 112 a covering the dorsal side.

When the hemostatic device 10 is mounted on the hand H of the patient, the portion 112 a covering the dorsal side of the hand faces the dorsal side Hb of the hand H of the patient. Moreover, when the hemostatic device 10 is mounted on the hand H of the patient, the portion 112 b covering the palm side of the hand faces the palm Hp of the hand H of the patient.

As illustrated in FIG. 2, in the bag body 120, in a state where the bag body 120 is disposed on the hand H of the patient and the pressing member 140 is not covering the puncture site t1, the puncture site t1 is exposed to an outside via the hole portion 115. Therefore, an operator such as a doctor can easily visually check the puncture site t1. Moreover, the support member 160 is disposed at a position facing the hole portion 115. Therefore, when the operator positions the hole portion 115 on the puncture site t1 on the dorsal side Hb of the hand H, the support member 160 is disposed on the palm Hp side of the hand H at a position overlapping the puncture site t1.

As illustrated in FIGS. 1 and 3, the pressing member 140 includes a pressing portion 141 configured to press the puncture site t1 and a position adjusting portion 145 which can adjust a position of the pressing portion 141 on the covering member 110.

The position adjusting portion 145 is formed of a belt-shaped member. A first end portion 145 a of the position adjusting portion 145 is fixed to the second region 112 of the bag body 120. Moreover, the position adjusting portion 145 has a second end portion 145 b on an opposite side of the pressing portion 141 with respect to the first end portion 145 a of the position adjusting portion 145.

The fixing member 150 is disposed on the second region 112 of the bag body 120. The fixing member 150 can fix the second end portion 145 b of the position adjusting portion 145. As illustrated in FIG. 1, the second end portion 145 b of the position adjusting portion 145 includes a fixing portion 146 which can be fixed to or separated from the fixing member 150. For example, the fixing portion 146 can be configured as the female side (or male side) of a surface fastener, and for example, the fixing member 150 can be configured as the male side (or female side) of the surface fastener. However, a specific structure of each of the fixing portion 146 and the fixing member 150 is not particularly limited as long as it has a structure which can be connected and separated. The fixing member 150 can be provided over a relatively wide range of the second region 112 of the bag body 120, for example.

When the operator mounts the hemostatic device 10 on the hand H of the patient, the operator can adjust the orientation of the position adjusting portion 145, a position at which the fixing portion 146 is fixed to the fixing member 150, or the like. Accordingly, the operator can easily adjust the orientation and the position of the pressing portion 141 provided in the position adjusting portion 145 with respect to the puncture site t1. For example, when the hemostatic device 10 is used to support hemostasis, in a case where the hand H of the patient is open or closed, the operator can freely adjust the position or the orientation of the pressing portion 141 according to the state of the hand H of the patient. Accordingly, it is possible to accurately adjust a position of the pressing portion 141 with respect to the puncture site t1.

Preferably, the position adjusting portion 145 is formed of a material having low elasticity so that the pressing portion 141 is prevented from being displaced from the puncture site t1 while the hemostatic device 10 is mounted on the hand H of the patient to support hemostasis.

As illustrated in FIGS. 1 and 5, the pressing portion 141 included in the pressing member 140 is an inflatable member (e.g., balloon) which can be inflated and deflated.

FIGS. 4 and 5 illustrate the pressing portion 141 which is inflated. An outer circumference of the inflated pressing portion 141 is smaller than an outer circumference of the support member 160. As used herein, the inflated state means a state where the pressing portion 141 is inflated while the hemostasis progresses with the support of the hemostatic device 10.

As illustrated in FIG. 5, the support member 160 is an inflatable member (e.g., balloon) which can be inflated and deflated. As described above, the outer circumference of the support member 160 is larger than that of the pressing portion 141. In a case that the pressing member 140 is a pressing member that does not inflate (for example, an elastic material such as sponge-like substances described above), a size relationship between the outer shape of the pressing member 140 and the outer shape of the support member 160 is defined by a comparison between the outer circumference of the pressing portion 141 in the state where the hemostasis is supported by the hemostatic device 10 and the outer circumference of the support member 160 in the state where the hemostasis is supported by the hemostatic device 10.

As illustrated in FIG. 5, the support member 160 is provided on an inner surface (a surface on a side facing the palm Hp of the hand H in the state where the hemostatic device 10 is mounted on the hand H) of the portion 112 b covering the palm side of the hand of the second region 112 of the bag body 120. The support member 160 faces the hole portion 115 of the second region 112 of the bag body 120. Accordingly, as illustrated in FIG. 1, the support member 160 can be viewed from the outside via the hole portion 115 in the state where the hand H of the patient is not inserted into the bag body 120. Preferably, a portion of the portion 112 b covering the palm side of the hand where the support member 160 is formed to be transparent, semi-transparent, or colored and transparent. The portion 112 b covering the palm side of the hand is formed in this way, and thus, the position of the support member 160 can be easily checked from the palm Hp side of the hand H.

As illustrated in FIG. 1, an injection portion 170 for inflating or deflating the pressing portion 141 is connected to the pressing portion 141.

As illustrated in FIGS. 1 and 5, the injection portion 170 includes a tube 171 which communicates with an inflatable space 141 a of the pressing portion 141 and has flexibility, a bag portion 172 which is disposed at one end portion of the tube 171 to communicate with a lumen of the tube 171, and a tubular connector 173 which houses a check valve (not illustrated) connected to the bag portion 172. When the operator or the like inflates the pressing portion 141, the operator inserts a tip tube portion of a syringe (not illustrated) into the connector 173 to open the check valve and pushes a plunger of the syringe to inject air in the syringe to the inflatable space 141 a of the pressing portion 141. When the pressing portion 141 is inflated by the above-described operation, the bag portion 172 which communicates with the inflatable space 141 a of the pressing portion 141 via the tube 171 is inflated. The operator checks the inflation of the bag portion 172, and thus, the operator can easily check visually that the pressing portion 141 can be pressurized without air leakage. The fluid used to inflate the pressing member 140 is not limited to air. Moreover, the tube 171 is liquid-tightly connected to the inflatable space 141 a of the pressing portion 141 via a connector (not illustrated).

As illustrated in FIG. 5, the pressing portion 141 is inflated in the state where the hemostatic device 10 is mounted on the hand H of the patient, and thus, the pressing portion 141 applies a compression force to the puncture site t1 formed on the hand H of the patient via the hole portion 115.

When the operator deflates the pressing portion 141 (or when the operator decreases the compression force of the pressing portion 141), the operator connects the syringe to the connector 173. The operator operates the syringe to discharge the air of the inflatable space 141 a of the pressing portion 141, and thus, the operator can deflate the pressing portion 141. The operator deflates the pressing portion 141 to decrease the compression force while hemostasis progresses with the support of the hemostatic device 10, and thus, it is possible to prevent occlusion of the blood vessel (for example, a distal radial artery of a hand).

As illustrated in FIG. 4, an injection portion 180 for inflating or deflating the support member 160 is connected to the support member 160. A fluid such as air flows into an inflatable space 160 a (refer to FIG. 5) of the support member 160 via a tube 181 of the injection portion 180, and thus, the support member 160 is inflated. Note that the injection portion 180 can be configured to be substantially the same as the injection portion 170, and thus, a detailed description of the injection portion 180 is omitted.

Each of the pressing member 140 and the support member 160 is not limited to the inflatable member (e.g., balloon). For example, as each of the pressing member 140 and the support member 160, it is possible to use a mechanical member in which an amount of pushing on the hand H is variable using an external operation such as rotation, a member configured to include a plastic resin material or gel for pushing the hand H so as to apply a surface pressure, a member including hydrophilic gel or a wound material (e.g., dressing material) to be brought into contact with the hand H, a member including gel which gradually reduces the compression force by decreasing water content with the lapse of time, an elastic material such as sponge-like substances, aggregates of fibers such as cotton (or any padding), metal, a member having a predetermined three-dimensional shape (e.g., spherical, ellipsoidal, or triangular pyramid shape), or a member obtained by appropriately combining these materials with each other.

The pressing portion 141 can be fixed to the position adjusting portion 145 by a known method such as adhesion or fusion. Moreover, the support member 160 can be fixed to the second region 112 of the bag body 120 by a known method such as adhesion or fusion.

As illustrated in FIG. 3, the position adjusting portion 145 includes a marker portion 147 for positioning the pressing member 140 so that the pressing member 140 is on top of the puncture site t1 when the hemostatic device 10 is mounted on the hand H of the patient. The marker portion 147 is disposed at a substantially central position of the pressing portion 141 in a plan view.

A specific shape and color of the marker portion 147, a method for forming the marker portion 147 in the position adjusting portion 145, or the like is not particularly limited. In addition, preferably, in the pressing member 140 and the position adjusting portion 145, a portion overlapping the marker portion 147 in a plan view and a periphery thereof are semitransparent or colored transparent. Accordingly, the operator can visually recognize the puncture site t1 from an outer surface side of the marker portion 147 even when the marker portion 147 is superposed on the puncture site t1.

For example, the marker portion 147 can be provided in the pressing member 140. When the pressing member 140 is the inflatable member, the marker portion 147 is provided on an inner surface of the pressing member 140 on a side close to the position adjusting portion 145 or on the inner surface of the pressing member 140 so that it is on a side spaced from the position adjusting portion 145. Accordingly, it is possible to prevent the marker portion 147 disposed in the pressing member 140 from coming into direct contact with the puncture site t1.

For example, each of the pressing member 140 and the support member 160 can be formed of polyolefin such as polyvinyl chloride, polyethylene, polypropylene, polybutadiene, and ethylene-vinyl acetate copolymer (EVA), polyester such as polyethylene terephthalate (PET) and polybutylene terephthalate (PBT), various thermoplastic elastomers such as polyvinylidene chloride, silicone, polyurethane, poly amide elastomer, polyurethane elastomer, and polyester elastomer, or any optional combination thereof (blend resin, polymer alloy, laminate, or the like).

Moreover, the first region 111 of the covering member 110 can be formed of polyolefin such as polyvinyl chloride, polyethylene, and polypropylene, polyester such as polyethylene terephthalate (PET) and polybutylene terephthalate (PBT), and a resin material such as silicone and urethane. For example, as the resin material of the first region 111, a material formed by producing chemical fibers from a resin material such as polyester and weaving the chemical fibers may be used. Moreover, the first region 111 of the covering member 110 can be formed of a material formed by weaving natural fibers such as cotton, silk, and wool. Preferably, the first region 111 is formed of a material having elasticity higher than that of the second region 112. Moreover, the third region 113 of the covering member 110 can be formed of the same material as that of the first region 111.

Preferably, the material of the first region 111 of the covering member 110 is hygroscopic. Specifically, it is preferable that the material of the first region 111 is a resin material that is hygroscopic or a material formed by weaving chemical fibers or natural fibers. For example, a material formed by weaving chemical fibers or natural fibers is hygroscopic when the material has a space between braided fibers. When the material of the first region 111 is hygroscopic, the first region 111 absorbs sweat or the like emitted from a skin of the hand H of the patient and is in close contact with the skin in the state where the hemostatic device 10 is mounted on the patient. Therefore, when the material of the first region 111 is hygroscopic, the hemostatic device 10 can prevent displacement of the pressing member 140 caused by the sweat.

Moreover, for example, as the material for the second region 112 of the covering member 110, polyamide, polyester such as polyethylene terephthalate (PET) and polybutylene terephthalate (PBT), polycarbonate, and a resin material such an ABS resin can be used. Preferably, the second region 112 is formed of a material having elasticity lower than that of the first region 111.

Next, an example of using the hemostatic device 10 will be described with reference to FIGS. 2 and 3. Hereinafter, a procedure of mounting the hemostatic device 10 on the hand H of the patient will be mainly described.

FIG. 2 illustrates a state when a medical device such as an introducer is inserted into the distal radial artery via the puncture site t1 formed on the dorsal side Hb of the hand H of the patient and various procedures are performed, and thereafter, the hemostasis of the puncture site t1 starts. Note that the medical device is not illustrated in FIGS. 2 and 3.

As illustrated in FIG. 2, the operator such as a doctor places the covering member 110 on the hand H of the patient. When the operator places the covering member 110 on the hand H of the patient, the hand H can be inserted from the third opening portion 123 formed in the third region 113 of the covering member 110. When the operator places the covering member 110 on the hand H, the operator enlarges the slit 116, and thus, the hand H can be easily inserted into the internal space 124 of the bag body 120.

The operator positions the hole portion 115 of the covering member 110 at the puncture site t1 formed on the dorsal side Hb of the hand H. The hole portion 115 is positioned at the puncture site t1 on the dorsal side Hb of the hand H, and the support member 160 is on the palm Hp side of the hand H to face the hole portion 115 with the dorsal side Hb of the hand H interposed therebetween.

Next, the operator positions the pressing portion 141 so that the pressing portion 141 overlaps the puncture site t1 from the dorsal side Hb of the hand H while the operator presses the support member 160 against the palm Hp of the hand H. Then, the operator fixes the fixing portion 146 formed in the second end portion 145 b of the position adjusting portion 145 to the fixing member 150 while the operator adjusts the orientation of the position adjusting portion 145, the position of the pressing portion 141 along the position adjusting portion 145, or the like. The operator can easily position the pressing portion 141 at the puncture site t1 by checking the positions of the puncture site t1 and the marker portion 147.

The operator can inflate the support member 160 before the operator disposes the pressing portion 141 at the puncture site t1. The operator inflates the support member 160, and thus, the operator can support the puncture site t1 from the palm Hp side of the hand H by the support member 160. Therefore, when the pressing portion 141 is positioned at the puncture site t1, it is possible to prevent the hemostatic device 10 from being displaced, and it is possible to easily position the pressing portion 141 at the puncture site t1. The support member 160 can be inflated using the injection portion 180 and the syringe (not illustrated).

Next, the operator inflates the pressing portion 141 using the injection portion 170 and the syringe (not illustrated). The pressing portion 141 is inflated, and thus, the pressing portion 141 applies the compression force to the puncture site t1. The operator removes the medical device such as the introducer from the puncture site t1 while the operator maintains the state in which the pressing portion 141 applies the compression force to the puncture site t1.

Effects of the hemostatic device 10 according to the present embodiment will be described.

The hemostatic device 10 according to the present embodiment includes the covering member 110 which includes the hole portion 115 at the puncture site t1 on the dorsal side Hb of the hand H of the patient, the pressing member 140 configured to apply compression force to the puncture site t1 in the state where the hole portion 115 is at the puncture site t1, the fixing member 150 configured to fix the pressing member 140 to the covering member 110 in the state where the pressing member 140 is disposed on the hole portion 115, and the support member 160 configured to support the hand H of the patient when the pressing member 140 applies the compression force to the puncture site t1. In the hemostatic device 10, at least a portion of the support member 160 faces the hole portion 115 with the dorsal side Hb of the hand H interposed therebetween, in the state where the covering member 110 is disposed on the dorsal side Hb of the hand H.

The hemostatic device 10 includes the support member 160 and the hole portion 115 which exists at the position facing the support member 160 with the dorsal side Hb of the hand H interposed therebetween. The support member 160 and the hole portion 115 exist at the positions facing each other with the dorsal side Hb of the hand H interposed therebetween. Accordingly, the operator presses the support member 160 to the hand H, and thus, the support member 160 supports the puncture site surrounded by the hole portion 115. Therefore, when the operator disposes the pressing member 140 at the puncture site t1 of the hand H, even in a case where the puncture site t1 exists in the hand H having many movable portions such as fingers, the support member 160 suppresses a movement in the vicinity of the puncture site t1. Therefore, the operator can easily mount the hemostatic device 10 on the patient and position the pressing member 140 at the puncture site t1 of the hand H. Moreover, in the hemostatic device 10, the support member 160 exists at the position facing the hole portion 115 in which the pressing member 140 is disposed. Accordingly, during hemostasis of the puncture site t1 of the hand H having many movable portions such as fingers, the support member 160 supports a force from the dorsal side Hb of the hand H caused by the pressing member 140, and thus, the support member 160 can suppress the displacement of the pressing member 140 caused by the movement of the hand H while supporting the compression force applied by the pressing member 140. Moreover, when the operator mounts the hemostatic device 10 on the patient, the hole portion 115 is at the position facing the support member 160. Accordingly, when the operator positions the hole portion 115 at the puncture site t1, the operator positions the support member 160 on the palm Hp side of the hand H in which the puncture site t1 is formed, and thus, the operator can easily mount the hemostatic device 10 on the patient.

Moreover, the covering member 110 is the bag body 120 that is arranged to wrap the entire dorsal side Hb of the hand H while being in contact with the dorsal side Hb of the hand H of the patient. The bag body 120 includes the first region 111 and the second region 112 which has elasticity lower than that of the first region 111. The second region 112 is arranged in a circumferential direction of the hand H of the patient passing through the hole portion 115. In the hemostatic device 10, since the covering member 110 is the bag body 120 which is arranged to wrap the entire dorsal side Hb of the hand H of the patient, an area which is in contact with the hand H of the patient is large. Therefore, even when the patient's hand H sweats in the state where the hemostatic device 10 is mounted on the hand H of the patient, displacement of the pressing member 140 due to the sweat can be prevented. Moreover, in the bag body 120, the second region 112 which has the elasticity lower than that of the first region 111 is arranged in the circumferential direction of the hand H of the patient passing through the hole portion 115. Accordingly, even when the patient moves the hand H while the hemostatic device 10 is mounted on the hand H of the patient to support hemostasis at the puncture site t1, it is possible to prevent the compression force applied to the puncture site t1 from decreasing which may have been otherwise caused by the second region 112 being expanded or extracted.

Moreover, the pressing member 140 is an inflatable member which is inflatable and deflatable, and the outer circumference of the inflatable member when inflated is smaller than the outer circumference of the support member 160. The pressing member 140 is locally supported from the palm Hp side of the hand H by the support member 160 in the state where the inflatable member applies the compression force to the puncture site t1, and thus, it is possible to more appropriately prevent the pressing member 140 from being displaced from the puncture site t1.

Moreover, the support member 160 is an inflatable member which is inflatable and deflatable. Accordingly, the operator can easily adjust the outer shape of the support member 160 or a support force for the pressing member 140 by inflating or deflating the support member 160.

Moreover, the pressing member 140 includes the pressing portion 141 configured to press the puncture site t1, and the position adjusting portion 145 which can adjust the position of the pressing portion 141 on the covering member 110. The first end portion 145 a of the position adjusting portion 145 is fixed to the second region 112 of the bag body 120. Accordingly, when the operator positions the pressing portion 141 at the puncture site t1, the operator adjusts the orientation or the like of the position adjusting portion 145 based on the first end portion 145 a of the position adjusting portion 145 fixed to the second region 112 of the bag body 120, and thus, the operator can appropriately position the pressing portion 141 at the puncture site t1. Moreover, the first end portion 145 a of the position adjusting portion 145 is fixed to the second region 112. Accordingly, even when the patient moves the hand H or the like, it is possible to prevent the movement of the position adjusting portion 145 caused by the expansion and contraction of the second region 112, and to prevent the position of the pressing portion 141 from deviating from the puncture site t1.

Moreover, the position adjusting portion 145 has the second end portion 145 b on an opposite side of the pressing portion 141 with respect to the first end portion 145 a of the position adjusting portion 145. The fixing member 150 is located in the second region 112 of the bag body 120 and the second end portion 145 b can be fixed to the second region 112 of the bag body 120. Accordingly, the operator can fix the covering member 110 to the hand H and position the pressing portion 141 disposed between the first end portion 145 a and the second end portion 145 b at the puncture site t1 by fixing the second end portion 145 b of the position adjusting portion 145 to the fixing member 150. In this case, since the second end portion 145 b of the position adjusting portion 145 is fixed to the second region 112 having the elasticity lower than that of the first region 111, it is possible to prevent the movement of the position adjusting portion 145 caused by the expansion and contraction of the second region 112, and to prevent the position of the pressing portion 141 from deviating from the puncture site t1.

Moreover, the covering member 110 has the slit 116, and the slit 116 connects the peripheral portion 117 of the covering member 110 to the hole portion 115. When the operator places the covering member 110 on the hand H, the operator enlarges the slit 116 so that the hand H can be easily inserted into the internal space 124 of the bag body 120. Moreover, since the slit 116 is connected to the hole portion 115, it is possible to widen the internal space 124 of the covering member 110 to the position where the hole portion 115 is formed. Accordingly, in the hemostatic device 10, the covering member 110 is more easily mounted on the hand H of the patient.

The covering member 110 includes the restriction member 118 which suppresses the enlargement of the slit 116. In the hemostatic device 10, the enlargement of the slit 116 can be suppressed by the restriction member 118. Accordingly, in the hemostatic device 10, it is possible to prevent the covering member 110 from being displaced due to careless enlargement of the slit 116 in the state where the hemostatic device 10 is disposed on the hand H of the patient.

Hereinbefore, the hemostatic device according to the present invention is described through the embodiment. However, the present invention is not limited to the configurations described in the specification, and may be appropriately changed based on the claims.

For example, in the descriptions of the embodiment, the hemostatic device for supporting hemostasis on the puncture site formed in the left hand is given as an example. However, the hemostatic device can be used to support hemostasis on a puncture site formed in the right hand. When the hemostatic device is used on the right hand, the shape of the covering member, the position of the pressing member, or the like can be appropriately changed to support hemostasis on the puncture site formed in the right hand.

Moreover, the shape (shape in a plan view) of the slit or the hole portion is not limited to the shapes described in the drawings, and can be appropriately changed. In addition, the specific shape of the covering member is not limited to the shape described in the drawings. For example, the covering member may have a glove shape which surrounds any finger including a thumb. 

What is claimed is:
 1. A hemostatic device comprising: a covering member configured to cover a dorsal side of a hand of a patient, the covering member including a hole portion through which a site on the dorsal side of the hand of the patient where bleeding is to be stopped, is to be exposed; a pressing member configured to apply a compression force to the site where the bleeding is to be stopped when the pressing member is positioned over the site and fixed to the covering member; a fixing member configured to fix the pressing member to the covering member; and a support member configured to support the hand of the patient when the pressing member applies the compression force to the site where the bleeding is to be stopped, wherein at least a portion of the support member faces the hole portion with the hand interposed therebetween, when the covering member is disposed on the dorsal side of the hand.
 2. The hemostatic device according to claim 1, wherein the covering member includes a bag body that is arranged to wrap around the hand, wherein the bag body includes a first region and a second region which has elasticity lower than that of the first region, and wherein the second region wraps around the hand of the patient and includes the hole portion.
 3. The hemostatic device according to claim 2, wherein the pressing member is an inflatable member which is inflatable and deflatable, and wherein an outer circumference of the inflatable member when inflated is smaller than an outer circumference of the support member.
 4. The hemostatic device according to claim 3, wherein the support member is an inflatable member which is inflatable and deflatable.
 5. The hemostatic device according to claim 2, wherein the pressing member includes a pressing portion that comes in contact with the site where the bleeding is to be stopped and is attached to a position adjusting portion which can adjust a position of the pressing portion on the covering member.
 6. The hemostatic device according to claim 5, wherein the position adjusting portion has a first end portion fixed to the second region and a second end portion that is on the opposite side of the pressing portion as the first end portion, and wherein the fixing member is located in the second region, and the second end portion is configured for attachment to and detachment from the fixing member.
 7. The hemostatic device according to claim 1, wherein the covering member has a slit that connects a peripheral portion of the covering member to the hole portion.
 8. The hemostatic device according to claim 7, wherein the covering member includes a restriction member which suppresses enlargement of the slit.
 9. A hemostatic device to be worn on a hand of a patient, comprising: a hand covering member having an opening at a proximal end thereof through which the hand is to be inserted and openings at a distal end thereof through which a thumb and fingers of the hand are to be inserted and exposed, the hand covering member including a proximal region at the proximal end, a distal region at the distal end, and a central region between the proximal region and the distal region, wherein the distal region is made of material having a first elasticity and the central region is made of material having a second elasticity that is lower than the first elasticity, and has a hole that exposes a part of the hand of the patient when the hemostatic device is worn on the hand of the patient; a pressing member attached to the hand covering member for covering the hole and configured to apply compression force to the exposed part of the hand of the patient; and a support member on the hand covering member on an opposite side of the hand with respect to the hole when the hemostatic device is worn on the hand of the patient.
 10. The hemostatic device according to claim 9, wherein the pressing member is fastened to the hand covering member when applying the compression force to the exposed part of the hand of the patient.
 11. The hemostatic device according to claim 10, wherein the pressing member is an inflatable member which is inflatable and deflatable, and wherein an outer circumference of the inflatable member when inflated is smaller than an outer circumference of the support member.
 12. The hemostatic device according to claim 11, wherein the support member is an inflatable member which is inflatable and deflatable.
 13. The hemostatic device according to claim 10, wherein the pressing member is mounted on an elastic strap having a first end that is fixed to the hand covering member and a second end that is configured for attachment to the hand covering member when detached from the hand covering member and for detachment from the hand covering member when attached to the hand covering member.
 14. The hemostatic device according to claim 9, wherein the proximal region has a slit that connects the opening at the proximal end to the hole.
 15. The hemostatic device according to claim 14, wherein the hand covering member includes a fastener configured to permit enlargement of the slit to facilitate insertion of the hand through the opening at the proximal end when an attachment end of the fastener is detached from the hand covering member, and to suppress enlargement of the slit when the attachment end of the fastener is attached to the hand covering member.
 16. A method of promoting hemostasis at a puncture site located on a dorsal side of a hand of a patient, said method comprising: inserting the hand of the patient through an opening at a proximal end of a hemostatic device until a thumb of the hand and fingers of the hand passes through openings at a distal end of the hemostatic device; positioning a hole formed through a cover of the hemostatic device so that the puncture site is exposed through the hole; positioning a loose end of a strap with respect to the cover of the hemostatic device so that a pressing member mounted on the strap is positioned on the hole and then attaching the loose end of the strap to the cover of the hemostatic device; and after attaching the loose end of the strap to the cover of the hemostatic device, applying compression force to the puncture site using the pressing member to promote hemostasis at the puncture site.
 17. The method according to claim 16, wherein the pressing member is an inflatable member which is inflated to apply the compression force to the puncture site.
 18. The method according to claim 17, wherein the hemostatic device has a support member on the cover thereof on an opposite side of the hand of the patient with respect to the hole, and wherein the support member is an inflatable member which is also inflated to apply the compression force to the puncture site.
 19. The method according to claim 18, wherein an outer circumference of the inflatable member of the pressing member when inflated is smaller than an outer circumference of the support member when inflated.
 20. The method according to claim 16, wherein the cover of the hemostatic device has a slit connecting the opening at the proximal end to the hole, and the slit enlarges to facilitate insertion of the hand through the opening at the proximal end. 